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作 者:吴静黎[1] 温帆渊[1] 杨小云[1] 李韶光[1] 李秋梅[1]
机构地区:[1]广东省惠州市中心人民医院,广东惠州516001
出 处:《河北医学》2007年第5期517-519,共3页Hebei Medicine
摘 要:目的:探讨缬沙坦对肝硬化患者血清血管紧张素Ⅱ(AngⅡ)转化生长因子-β1(TGF-β1)的影响及意义。方法:40例肝硬化患者被随机分为治疗组和对照组各20例,两组均给予常规治疗,治疗组在常规治疗基础上加用缬沙坦80mg/d,于治疗前及治疗6个月时采用ELISA法检测血清AngⅡ、TGF-β1。结果:治疗前肝硬化患者血清AngⅡ(167.84±64.81vs 51.13±15.95pg/l)及TGFβ1(181.12±32.63 vs31.46±10.39μg/l)水平均明显高于健康人,应用缬沙坦治疗后血清AngⅡ(168.67±69.03vs218.46±74.79 pg/l)较治疗前升高,而血清TGFβ1(182.22±30.60vs121.77±13.84μg/l)较治疗前下降,差异均有显著性。结论:血管紧张素ⅡⅠ型受体拮抗剂缬沙坦能降低血清TGFβ1水平,具有一定的抗纤维化作用。Objective: To investigate the influence and clinical effect of valsartan on liver cirrhosis in serum Ang Ⅱ and TGF- β1. Method: 40 liver cirrhsis patients were randomly divided into two groups : treatment group and control group,20 cases in each group. The control group was treated with routine treatment,the treatment group,besides routine with treatment ,was added valsartan 80mg/day . Before treatment and after 6 months ELISA techniques were used to detect the levels of serum Ang Ⅱ and TGFβ1 in 40 patients with liver cirrhosis . Result: Before treatment the levels of serum Ang Ⅱ ( 167.84 ±64.81vs 51.13 ± 15.95pg/1) and TGF - β1 ( 181.12 ± 32.63 vs31.46 ±10.39μg/1) in liver cirrhosis were significantly higher than that in health peason, After treated with valsartan , serum Ang Ⅱ ( 168.67 ± 69.03vs218.46 ± 74.79 pg/1) in after treatment 6 months was significantly higher than that before treatment , but TGF - β1 ( 182.22 ±30.60vs121.77 ± 13.84μg/1) was lower significantly than that before. Conclusion: Angiotensin Ⅱ type Ⅰ receptor blocker valsartan can reduce the levels of serum TGFβ1, it can retard the progression of hepatic fibrosis.
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